What is the correct IUPAC name of the following compound?

- A
4-Ethyl-1-hydroxycyclopent-2-ene
- B
1-Ethyl-3-hydroxycyclopent-2-ene
- C
1-Ethylcyclopent-2-en-3-ol
- D
4-Ethylcyclopent-2-en-1-ol
What is the correct IUPAC name of the following compound?

4-Ethyl-1-hydroxycyclopent-2-ene
1-Ethyl-3-hydroxycyclopent-2-ene
1-Ethylcyclopent-2-en-3-ol
4-Ethylcyclopent-2-en-1-ol
Correct answer:D
Standard Method
Given: A cyclic compound containing a cyclopentene ring, one hydroxyl group and one ethyl group.
Find: The correct IUPAC name.
For cyclic compounds, numbering starts from the carbon bearing the highest-priority functional group. Here, -OH has higher priority than the double bond, so the carbon attached to -OH gets locant .
The ring is then numbered to give the double bond the lowest possible locant. This places the double bond at , giving the parent name cyclopent-2-en-1-ol.
The ethyl substituent is then found at carbon .
Therefore, the correct IUPAC name is 4-Ethylcyclopent-2-en-1-ol. The correct option is D.
Stepwise Naming
Given: The structure is a cyclopentene ring with a double bond, an ethyl substituent, and a hydroxyl group.
Find: The systematic IUPAC name.
Hence, the full name becomes 4-Ethylcyclopent-2-en-1-ol.
The solution notes the same final result, although it mistakenly mentions a cyclohexene structure in one sentence. The derived name from the working remains 4-Ethylcyclopent-2-en-1-ol.
Giving the double bond higher numbering priority than the -OH group. This is wrong because alcohol is the principal functional group here. Start numbering from the carbon attached to -OH.
Using the form hydroxy in the parent name instead of the suffix -ol. This is wrong because the hydroxyl group is the principal functional group, so it must be written as the suffix -ol.
Choosing the wrong numbering direction around the ring. This gives incorrect locants for the double bond or substituent. After assigning to the -OH carbon, number the ring to give the double bond the lowest possible number.
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